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  • enthalpy has been found for systems that form 1:1 complexes by hydrogen bonding. Starting from relatively general assumptions, we havederived two forms of this relation. The first form is represented by proportionality between the solution enthalpy of the proton-donor and the chemical shift change of its active hydrogen atom. The second form is mediated by the relative extent of hydrogen bond formation , a quantity which can be directly evaluated from measurements of either the 1H NMR chemical shift orthe mixing enthalpy. The validity of both relation forms has been convincingly demonstrated for 12 systems formed by a strong proton donor (halothane [1-brom-1-chlor-2,2,2-trifluorethane] or trichloromethane) and an oxygen- or nitrogen-containing proton -acceptor (aliphatic
  • enthalpy has been found for systems that form 1:1 complexes by hydrogen bonding. Starting from relatively general assumptions, we havederived two forms of this relation. The first form is represented by proportionality between the solution enthalpy of the proton-donor and the chemical shift change of its active hydrogen atom. The second form is mediated by the relative extent of hydrogen bond formation , a quantity which can be directly evaluated from measurements of either the 1H NMR chemical shift orthe mixing enthalpy. The validity of both relation forms has been convincingly demonstrated for 12 systems formed by a strong proton donor (halothane [1-brom-1-chlor-2,2,2-trifluorethane] or trichloromethane) and an oxygen- or nitrogen-containing proton -acceptor (aliphatic (en)
Title
  • A simple relation between 1H NMR data and mixing enthalpy for systems with complex formation by hydrogen bonding
  • A simple relation between 1H NMR data and mixing enthalpy for systems with complex formation by hydrogen bonding (en)
skos:prefLabel
  • A simple relation between 1H NMR data and mixing enthalpy for systems with complex formation by hydrogen bonding
  • A simple relation between 1H NMR data and mixing enthalpy for systems with complex formation by hydrogen bonding (en)
skos:notation
  • RIV/60461373:22340/02:00006952!RIV/2004/MSM/223404/N
http://linked.open.../vavai/riv/strany
  • 12307-12310
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • Z(MSM 223400008)
http://linked.open...iv/cisloPeriodika
  • 47
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
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http://linked.open...dnocenehoVysledku
  • 637212
http://linked.open...ai/riv/idVysledku
  • RIV/60461373:22340/02:00006952
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • 1H NMR; mixing enthalpy; hydrogen bonding (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • US - Spojené státy americké
http://linked.open...ontrolniKodProRIV
  • [425DD162129A]
http://linked.open...i/riv/nazevZdroje
  • Jornal of Physical Chemistry B
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...ocetUcastnikuAkce
http://linked.open...nichUcastnikuAkce
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 106
http://linked.open...iv/tvurceVysledku
  • Tkadlecová, Marcela
  • Dohnal, Vladimír
http://linked.open...n/vavai/riv/zamer
issn
  • 1520-6106
number of pages
http://localhost/t...ganizacniJednotka
  • 22340
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